Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005657 | replication fork | 2 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0035861 | site of double-strand break | 3 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
GO:0090734 | site of DNA damage | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HBR0
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 7 |
GO:0006259 | DNA metabolic process | 4 | 7 |
GO:0006281 | DNA repair | 5 | 7 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 7 |
GO:0006807 | nitrogen compound metabolic process | 2 | 7 |
GO:0006950 | response to stress | 2 | 7 |
GO:0006974 | DNA damage response | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0033554 | cellular response to stress | 3 | 7 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 7 |
GO:0043170 | macromolecule metabolic process | 3 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 7 |
GO:0046483 | heterocycle metabolic process | 3 | 7 |
GO:0050896 | response to stimulus | 1 | 7 |
GO:0051716 | cellular response to stimulus | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0090304 | nucleic acid metabolic process | 4 | 7 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 7 |
GO:0000731 | DNA synthesis involved in DNA repair | 6 | 1 |
GO:0006301 | postreplication repair | 6 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009314 | response to radiation | 3 | 1 |
GO:0009628 | response to abiotic stimulus | 2 | 1 |
GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
GO:0019985 | translesion synthesis | 7 | 1 |
GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
GO:0042276 | error-prone translesion synthesis | 8 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
GO:0071897 | DNA biosynthetic process | 5 | 1 |
GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 7 |
GO:0003677 | DNA binding | 4 | 7 |
GO:0003684 | damaged DNA binding | 5 | 7 |
GO:0005488 | binding | 1 | 7 |
GO:0097159 | organic cyclic compound binding | 2 | 7 |
GO:1901363 | heterocyclic compound binding | 2 | 7 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003887 | DNA-directed DNA polymerase activity | 5 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
GO:0034061 | DNA polymerase activity | 4 | 1 |
GO:0140097 | catalytic activity, acting on DNA | 3 | 1 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 594 | 598 | PF00656 | 0.639 |
CLV_NRD_NRD_1 | 150 | 152 | PF00675 | 0.312 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.302 |
CLV_NRD_NRD_1 | 357 | 359 | PF00675 | 0.792 |
CLV_NRD_NRD_1 | 364 | 366 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 368 | 370 | PF00675 | 0.611 |
CLV_PCSK_FUR_1 | 365 | 369 | PF00082 | 0.624 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.312 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.302 |
CLV_PCSK_KEX2_1 | 357 | 359 | PF00082 | 0.677 |
CLV_PCSK_KEX2_1 | 366 | 368 | PF00082 | 0.619 |
CLV_PCSK_KEX2_1 | 545 | 547 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 66 | 68 | PF00082 | 0.302 |
CLV_PCSK_PC1ET2_1 | 366 | 368 | PF00082 | 0.633 |
CLV_PCSK_PC1ET2_1 | 545 | 547 | PF00082 | 0.582 |
CLV_PCSK_PC1ET2_1 | 66 | 68 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 119 | 123 | PF00082 | 0.280 |
CLV_PCSK_SKI1_1 | 235 | 239 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 369 | 373 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.214 |
CLV_Separin_Metazoa | 203 | 207 | PF03568 | 0.502 |
CLV_Separin_Metazoa | 426 | 430 | PF03568 | 0.468 |
DEG_APCC_DBOX_1 | 149 | 157 | PF00400 | 0.577 |
DEG_APCC_DBOX_1 | 368 | 376 | PF00400 | 0.454 |
DEG_COP1_1 | 523 | 532 | PF00400 | 0.475 |
DEG_SPOP_SBC_1 | 384 | 388 | PF00917 | 0.467 |
DOC_CYCLIN_RxL_1 | 232 | 243 | PF00134 | 0.502 |
DOC_CYCLIN_yCln2_LP_2 | 724 | 730 | PF00134 | 0.514 |
DOC_MAPK_gen_1 | 453 | 461 | PF00069 | 0.566 |
DOC_MAPK_RevD_3 | 167 | 183 | PF00069 | 0.469 |
DOC_PP2B_LxvP_1 | 286 | 289 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 724 | 727 | PF13499 | 0.635 |
DOC_PP2B_LxvP_1 | 729 | 732 | PF13499 | 0.585 |
DOC_PP4_FxxP_1 | 201 | 204 | PF00568 | 0.502 |
DOC_PP4_FxxP_1 | 297 | 300 | PF00568 | 0.436 |
DOC_PP4_FxxP_1 | 676 | 679 | PF00568 | 0.533 |
DOC_PP4_FxxP_1 | 728 | 731 | PF00568 | 0.511 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 691 | 695 | PF00917 | 0.588 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 6 | 11 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 631 | 636 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 658 | 663 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 687 | 692 | PF00397 | 0.529 |
DOC_WW_Pin1_4 | 732 | 737 | PF00397 | 0.650 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.556 |
LIG_14-3-3_CanoR_1 | 193 | 198 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 291 | 300 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 367 | 375 | PF00244 | 0.504 |
LIG_14-3-3_CanoR_1 | 420 | 426 | PF00244 | 0.490 |
LIG_14-3-3_CanoR_1 | 429 | 435 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 453 | 458 | PF00244 | 0.529 |
LIG_14-3-3_CanoR_1 | 539 | 547 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 553 | 558 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 70 | 77 | PF00244 | 0.396 |
LIG_Actin_WH2_2 | 606 | 621 | PF00022 | 0.479 |
LIG_APCC_ABBAyCdc20_2 | 250 | 256 | PF00400 | 0.460 |
LIG_BRCT_BRCA1_1 | 219 | 223 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 293 | 297 | PF00533 | 0.407 |
LIG_BRCT_BRCA1_1 | 414 | 418 | PF00533 | 0.460 |
LIG_BRCT_BRCA1_1 | 7 | 11 | PF00533 | 0.413 |
LIG_eIF4E_1 | 232 | 238 | PF01652 | 0.502 |
LIG_FHA_1 | 174 | 180 | PF00498 | 0.462 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.429 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.454 |
LIG_FHA_1 | 420 | 426 | PF00498 | 0.490 |
LIG_FHA_1 | 474 | 480 | PF00498 | 0.457 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.490 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.450 |
LIG_FHA_1 | 623 | 629 | PF00498 | 0.634 |
LIG_FHA_1 | 632 | 638 | PF00498 | 0.625 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.477 |
LIG_FHA_1 | 652 | 658 | PF00498 | 0.444 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.543 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.490 |
LIG_FHA_2 | 539 | 545 | PF00498 | 0.503 |
LIG_FHA_2 | 683 | 689 | PF00498 | 0.697 |
LIG_FHA_2 | 739 | 745 | PF00498 | 0.547 |
LIG_LIR_Apic_2 | 294 | 300 | PF02991 | 0.363 |
LIG_LIR_Apic_2 | 327 | 332 | PF02991 | 0.420 |
LIG_LIR_Apic_2 | 673 | 679 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 139 | 149 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.460 |
LIG_LIR_Gen_1 | 430 | 439 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 441 | 450 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 387 | 393 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 415 | 421 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 430 | 434 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 441 | 446 | PF02991 | 0.456 |
LIG_MYND_1 | 727 | 731 | PF01753 | 0.510 |
LIG_PAM2_1 | 719 | 731 | PF00658 | 0.506 |
LIG_PCNA_yPIPBox_3 | 549 | 562 | PF02747 | 0.593 |
LIG_PTB_Apo_2 | 460 | 467 | PF02174 | 0.520 |
LIG_SH2_NCK_1 | 28 | 32 | PF00017 | 0.460 |
LIG_SH2_PTP2 | 142 | 145 | PF00017 | 0.502 |
LIG_SH2_SRC | 142 | 145 | PF00017 | 0.502 |
LIG_SH2_SRC | 96 | 99 | PF00017 | 0.381 |
LIG_SH2_STAP1 | 259 | 263 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.413 |
LIG_SH3_3 | 168 | 174 | PF00018 | 0.460 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.551 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.460 |
LIG_SH3_3 | 666 | 672 | PF00018 | 0.671 |
LIG_SH3_3 | 712 | 718 | PF00018 | 0.760 |
LIG_SH3_3 | 724 | 730 | PF00018 | 0.575 |
LIG_SH3_4 | 280 | 287 | PF00018 | 0.378 |
LIG_SUMO_SIM_anti_2 | 422 | 430 | PF11976 | 0.403 |
LIG_SUMO_SIM_anti_2 | 623 | 634 | PF11976 | 0.650 |
LIG_SUMO_SIM_anti_2 | 747 | 757 | PF11976 | 0.601 |
LIG_SUMO_SIM_par_1 | 166 | 173 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 284 | 290 | PF11976 | 0.429 |
LIG_SUMO_SIM_par_1 | 473 | 481 | PF11976 | 0.513 |
LIG_SUMO_SIM_par_1 | 609 | 615 | PF11976 | 0.567 |
LIG_SUMO_SIM_par_1 | 623 | 634 | PF11976 | 0.546 |
LIG_SUMO_SIM_par_1 | 653 | 661 | PF11976 | 0.508 |
LIG_SUMO_SIM_par_1 | 80 | 86 | PF11976 | 0.484 |
LIG_TRAF2_1 | 686 | 689 | PF00917 | 0.655 |
LIG_WRC_WIRS_1 | 558 | 563 | PF05994 | 0.574 |
LIG_WW_3 | 730 | 734 | PF00397 | 0.539 |
MOD_CDC14_SPxK_1 | 690 | 693 | PF00782 | 0.528 |
MOD_CDK_SPxK_1 | 687 | 693 | PF00069 | 0.531 |
MOD_CDK_SPxxK_3 | 83 | 90 | PF00069 | 0.351 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.451 |
MOD_CK1_1 | 430 | 436 | PF00069 | 0.293 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.328 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.520 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.561 |
MOD_CK1_1 | 598 | 604 | PF00069 | 0.577 |
MOD_CK1_1 | 612 | 618 | PF00069 | 0.465 |
MOD_CK1_1 | 658 | 664 | PF00069 | 0.560 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.622 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.336 |
MOD_CK1_1 | 734 | 740 | PF00069 | 0.629 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.492 |
MOD_CK2_1 | 383 | 389 | PF00069 | 0.435 |
MOD_CK2_1 | 420 | 426 | PF00069 | 0.351 |
MOD_CK2_1 | 538 | 544 | PF00069 | 0.661 |
MOD_CK2_1 | 584 | 590 | PF00069 | 0.510 |
MOD_CK2_1 | 658 | 664 | PF00069 | 0.636 |
MOD_CK2_1 | 682 | 688 | PF00069 | 0.753 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.487 |
MOD_GlcNHglycan | 260 | 264 | PF01048 | 0.309 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.388 |
MOD_GlcNHglycan | 293 | 296 | PF01048 | 0.355 |
MOD_GlcNHglycan | 301 | 304 | PF01048 | 0.447 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.198 |
MOD_GlcNHglycan | 469 | 472 | PF01048 | 0.180 |
MOD_GlcNHglycan | 577 | 580 | PF01048 | 0.682 |
MOD_GlcNHglycan | 586 | 589 | PF01048 | 0.636 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.614 |
MOD_GlcNHglycan | 737 | 740 | PF01048 | 0.673 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.367 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.575 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.499 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.349 |
MOD_GSK3_1 | 430 | 437 | PF00069 | 0.464 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.313 |
MOD_GSK3_1 | 507 | 514 | PF00069 | 0.358 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.600 |
MOD_GSK3_1 | 549 | 556 | PF00069 | 0.651 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.623 |
MOD_GSK3_1 | 651 | 658 | PF00069 | 0.566 |
MOD_GSK3_1 | 670 | 677 | PF00069 | 0.666 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.704 |
MOD_GSK3_1 | 709 | 716 | PF00069 | 0.538 |
MOD_GSK3_1 | 731 | 738 | PF00069 | 0.690 |
MOD_LATS_1 | 451 | 457 | PF00433 | 0.275 |
MOD_LATS_1 | 551 | 557 | PF00433 | 0.595 |
MOD_N-GLC_1 | 598 | 603 | PF02516 | 0.770 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.455 |
MOD_NEK2_1 | 3 | 8 | PF00069 | 0.491 |
MOD_NEK2_1 | 408 | 413 | PF00069 | 0.315 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.422 |
MOD_NEK2_1 | 557 | 562 | PF00069 | 0.582 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.611 |
MOD_NEK2_1 | 674 | 679 | PF00069 | 0.549 |
MOD_PK_1 | 693 | 699 | PF00069 | 0.533 |
MOD_PKA_1 | 367 | 373 | PF00069 | 0.552 |
MOD_PKA_1 | 66 | 72 | PF00069 | 0.336 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.367 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.544 |
MOD_PKA_2 | 419 | 425 | PF00069 | 0.360 |
MOD_PKA_2 | 538 | 544 | PF00069 | 0.576 |
MOD_PKA_2 | 568 | 574 | PF00069 | 0.550 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.719 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.348 |
MOD_PKB_1 | 365 | 373 | PF00069 | 0.547 |
MOD_Plk_1 | 399 | 405 | PF00069 | 0.458 |
MOD_Plk_1 | 444 | 450 | PF00069 | 0.351 |
MOD_Plk_1 | 598 | 604 | PF00069 | 0.505 |
MOD_Plk_1 | 623 | 629 | PF00069 | 0.627 |
MOD_Plk_1 | 92 | 98 | PF00069 | 0.198 |
MOD_Plk_2-3 | 751 | 757 | PF00069 | 0.684 |
MOD_Plk_4 | 282 | 288 | PF00069 | 0.373 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.257 |
MOD_Plk_4 | 408 | 414 | PF00069 | 0.296 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.236 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.367 |
MOD_Plk_4 | 553 | 559 | PF00069 | 0.585 |
MOD_Plk_4 | 624 | 630 | PF00069 | 0.676 |
MOD_Plk_4 | 670 | 676 | PF00069 | 0.529 |
MOD_Plk_4 | 719 | 725 | PF00069 | 0.576 |
MOD_Plk_4 | 751 | 757 | PF00069 | 0.666 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.367 |
MOD_ProDKin_1 | 6 | 12 | PF00069 | 0.525 |
MOD_ProDKin_1 | 631 | 637 | PF00069 | 0.688 |
MOD_ProDKin_1 | 658 | 664 | PF00069 | 0.655 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.607 |
MOD_ProDKin_1 | 687 | 693 | PF00069 | 0.531 |
MOD_ProDKin_1 | 732 | 738 | PF00069 | 0.652 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.443 |
TRG_DiLeu_BaEn_1 | 234 | 239 | PF01217 | 0.367 |
TRG_DiLeu_BaLyEn_6 | 174 | 179 | PF01217 | 0.367 |
TRG_ENDOCYTIC_2 | 142 | 145 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 254 | 257 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 28 | 31 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 443 | 446 | PF00928 | 0.330 |
TRG_ER_diArg_1 | 249 | 252 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 365 | 368 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 452 | 455 | PF00400 | 0.351 |
TRG_NES_CRM1_1 | 14 | 25 | PF08389 | 0.383 |
TRG_NES_CRM1_1 | 481 | 495 | PF08389 | 0.351 |
TRG_NLS_MonoCore_2 | 364 | 369 | PF00514 | 0.582 |
TRG_NLS_MonoExtC_3 | 357 | 362 | PF00514 | 0.671 |
TRG_NLS_MonoExtC_3 | 364 | 369 | PF00514 | 0.606 |
TRG_NLS_MonoExtN_4 | 357 | 362 | PF00514 | 0.658 |
TRG_NLS_MonoExtN_4 | 365 | 370 | PF00514 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 151 | 155 | PF00026 | 0.381 |
TRG_Pf-PMV_PEXEL_1 | 177 | 181 | PF00026 | 0.367 |
TRG_Pf-PMV_PEXEL_1 | 591 | 595 | PF00026 | 0.532 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEU7 | Leptomonas seymouri | 55% | 95% |
A4HZ62 | Leishmania infantum | 78% | 100% |
D0A1I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E8NHQ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 76% | 100% |
Q4QCF2 | Leishmania major | 79% | 100% |
Q8H2D5 | Arabidopsis thaliana | 28% | 100% |